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13C NMR (126 MHz, dmso) ¦Ä 10.70,18.52,29.91,30.13, 36.60, 43.18,43.95, 56.08, 69.72,70.74, 80.32,106.43, 111.71, 126.31, 128.73, 128.92,131.74, 132.12, 132.94, 133.791, 37.62, 139.66,143.82, 157.68,167.87.
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wangcong123: ½ð±Ò+20, ¡ïÓаïÖú 2015-03-27 21:32:32
1 .     trienomycinol
    ÏàËÆ¶È:69.2%
The Journal of Antibiotics          1988          41          1223-1230
STRUCTURE-ACTIVITY RELATIONSHIP OF A NOVEL ANTITUMOR ANSAMYCIN ANTIBIOTIC TRIENOMYCIN A AND RELATED COMPOUNDS
SHINJI FUNAYAMA, YUMI ANRAKU, AKIRA MITA, Zm-Bo YANG, KIYOSHI SHIBATA, KANKI KOMIYAMA, IWAO UMEZAWA, SATOSHI OMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     4-hydroxy-4-{9-hydroxy-9-[2-(1-hydroxy-6-methyl-octa-2,4-dienylidene)-3,6-dioxo-cyclohexylidene]-nona-1,3,5,7-tetraenyl}-6-oxa-bicyclo[3.1.0]hex-2-ene-2-carboxylic acid
C30H32O8     ÏàËÆ¶È:61.5%
Microbiological Research          2013          168          223-230
Taxonomy and chemical characterization of new antibiotics produced by Saccharothrix SA198 isolated from a Saharan soil
D. Boubetra, N. Sabaou, A. Zitouni, C. Bijani, A. Lebrihi, F. Mathieu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     17¦Â-(1-phenyl-5-pyrazolyl)androst-5-en-3¦Â-ol
C28H36N2O     ÏàËÆ¶È:56%
Steroids          2010          75          450-456
Synthesis of regioisomeric 17¦Â-N-phenylpyrazolyl steroid derivatives and their inhibitory effect on 17¦Á-hydroxylase/C17,20-lyase
Zolt¨¢n Iv¨¢nyi, J¨¢nos Wölfling, Tam¨¢s Görbe, Mih¨¢ly Sz¨¦csi, Tibor Wittmann, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (S)-6¦Â-NH-Ts-7¦Â-Methoxy-7,8-dihydro disinomenine
C52H66N4O10S2     ÏàËÆ¶È:56%
Bioorganic & Medicinal Chemistry          2011          19          3096-3104
Synthesis and biological evaluation of unique stereodimers of sinomenine analogues as potential inhibitors of NO production
Peng Teng,Hai-Liang Liu, Zhang-Shuang Deng, Zhi-Bing Shi ,Yun-Mian He , Li-Li Feng,Qiang Xu ,Jian-Xin Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3-Methoxy-17a-(N-phenylcarboxamido)-13¦Á-D-homoestra-1,3,5(10),17-tetraene
C27H31O2N     ÏàËÆ¶È:56%
Steroids          2010          75          1075-1081
Novel 13¦Â- and 13¦Á-d-homo steroids: 17a-carboxamido-d-homoestra-1,3,5(10),17-tetraene derivatives via palladium-catalyzed aminocarbonylations
Attila Tak¨¢cs, P¨¦ter ¨¢cs, Zolt¨¢n Berente, J¨¢nos Wölfling, Gyula Schneider, L¨¢szl¨® Koll¨¢r
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     comopund XviI
C24H20O6     ÏàËÆ¶È:56%
Russian Journal of Organic Chemistry          2001          37          1276-1283
Cycloaddition of 1-Aryl-3-trimethylsiloxy-1,3-butadienes in the Synthesis of Natural Quinone Analogs
I. V. Nechepurenko, E. E. Shul'ts and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (1E,5R,8R)-8-O-[(Z)-p-coumaroyl]-5-hydroxyhumula-1(10),4-(15)-dien-8-ol
C24H32O4     ÏàËÆ¶È:56%
Organic & Biomolecular Chemistry          2013          11          4840-4846
Humulane-type sesquiterpenoids from Pilea cavaleriei subsp. crenata
Cang-Song Liao, Chun-Ping Tang, Sheng Yao and Yang Ye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     3-O-(4-Methoxybenzyl)-¦Â-estradiol
C26H32O3     ÏàËÆ¶È:56%
Tetrahedron          2014          70          1975-1983
Proton-exchanged montmorillonite-mediated reactions of methoxybenzyl esters and ethers
Dongyin Chen, Chang Xu, Jie Deng, Chunhuan Jiang, Xiaoan Wen, Lingyi Kong, Ji Zhang, Hongbin Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     reblastatin
C28H42N2O8     ÏàËÆ¶È:55.5%
The Journal of Antibiotics          2000          53          657-663
Discovery of Novel Ansamycins Possessing Potent Inhibitory Activity in a Cell-based Oncostatin M Signalling Assay
PAUL STEAD,SHAZIA LATIF,ANDREW P. BLACKABY,PHILIP J. SIDEBOTTOM,ANGELA DEAKIN,NICHOLAS L. TAYLOR,PAUL LIFE,JOHN SPAULL,FIONA BURRELL,ROSIE JONES,JANE LEWIS,IAN DAVIDSON and THOMAS MANDER
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     biselyngbyolide A
C27H42O5     ÏàËÆ¶È:55.5%
Chemistry Letters          2012          41          165-167
Biselyngbyolide A, a Novel Cytotoxic Macrolide from the Marine Cyanobacterium Lyngbya sp.
Maho Morita, Osamu Ohno, and Kiyotake Suenaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     17¦Â-estradiol-3-benzyl ether 17-tosylate
C32H36O4S     ÏàËÆ¶È:55.5%
Steroids          2011          76          1141-1148
Synthesis of novel steroidal 17 -triazolyl derivatives via Cu(I)-catalyzed azide-alkyne cycloaddition, and an evaluation of their cytotoxic activity in vitro
¨¦va Frank∗, Judit Moln¨¢r, Istv¨¢n Zupk¨®, Zal¨¢n K¨¢d¨¢r, J¨¢nos Wölfling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     17-O-demethyllebstatin
    ÏàËÆ¶È:55.5%
China Journal of Chinese Materia Medica          2011          36          1763-1768
Isolation and structural elucidation of secondary metabolites from marine Streptomyces sp. SCSIO 1934
NIU, Siwen, LI, Sumei, TIAN, Xinpeng, HU, Tao, JU, Jianhua, YNAG, Xiaohong, ZHANG, Si, ZHANG, Changsheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     biselyngbyolide B
C27H40O4     ÏàËÆ¶È:55.5%
Chemistry Letters          2014          43          287-289
Biselyngbyolide B, a Novel ER Stress-inducer Isolated from the Marine Cyanobacterium Lyngbya sp.
Osamu Ohno, Ayane Watanabe, Maho Morita, and Kiyotake Suenaga*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ((2'R,8S,9S,13S,14S,16S,17R)-16-chloro-3-methoxy-13-methyl-6,7,8,9,11,12,13,14,15,16-decahydrospiro[cyclopenta[a]phenanthrene-17,1'-cyclopropan]-2'-yl)methyl benzoate
C29H33ClO3     ÏàËÆ¶È:55.5%
Tetrahedron          2015          71          233−244
Synthesis of steroidal derivatives bearing a small ring using a catalytic [2+2] cycloaddition and a ring-contraction rearrangement
Norihito Arichi, Kenji Hata, Yoshiji Takemoto, Ken-ichi Yamada, Yousuke Yamaoka, Kiyosei Takasu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (E)-(1S,5R,9R,11R,12R,13S)-5-[(1E,3E)-6-((1S,2R)-2-chlorocyclopropyl)hexa-1,3-dien-5-ynyl]-1,13-dihydroxy-9-methoxy-7,10,12-tri-methyl-4,15-dioxabicyclo[9.3.1]pentadec-7-en-3-one
C26H35ClO6     ÏàËÆ¶È:53.8%
Journal of the American Chemical Society          2002          124          10396-10415
Callipeltoside A: Total Synthesis, Assignment of the Absolute and Relative Configuration, and Evaluation of Synthetic Analogues
Barry M. Trost, Janet L. Gunzner, Olivier Dirat, and Young H. Rhee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (E)-(1S,5R,9R,11R,12R,13S)-5-[(1E,3E)-6-((1R,2S)-2-chlorocyclo-propyl)hexa-1,3-dien-5-ynyl]-1,13-dihydroxy-9-methoxy-7,10,12-tri-methyl-4,15-dioxabicyclo[9.3.1]pentadec-7-en-3-one
C26H35ClO6     ÏàËÆ¶È:53.8%
Journal of the American Chemical Society          2002          124          10396-10415
Callipeltoside A: Total Synthesis, Assignment of the Absolute and Relative Configuration, and Evaluation of Synthetic Analogues
Barry M. Trost, Janet L. Gunzner, Olivier Dirat, and Young H. Rhee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     compound 31
    ÏàËÆ¶È:53.8%
Angewandte Chemie International Edition          2001          40          603-607
Total Synthesis of the Callipeltoside Aglycon
Ian Paterson, Robert D. M. Davies, and Rodolfo Marquez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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